Abstract
Hairy cell leukemia variant (HCL-v) is a rare form of a chronic B-cell lymphoproliferative disorder. Unlike typical hairy cell leukemia (HCL) where the complete response (CR) rate to 2-chlorodeoxyadenosine and 2'-deoxycoformycin can approach about 90%, in HCL-v CR is rare and partial response (PR) occurs in approximately 50% with these agents. Rituximab treatment in relapsed or refractory HCL results in a CR of 13% to 53%, but its use in HCL-v has not been reported in the literature to our knowledge. We describe a patient with HCL-v, whose course was previously complicated by pure red cell aplasia who achieved CR after treatment with rituximab. We also briefly review outcomes of treatments used in HCL-v reported in the current literature.
MeSH terms
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2-Chloroadenosine / administration & dosage
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2-Chloroadenosine / analogs & derivatives
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Aged
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Antibodies, Monoclonal / therapeutic use*
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Antibodies, Monoclonal, Murine-Derived
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Antineoplastic Agents / therapeutic use*
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use
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Blood Transfusion
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Combined Modality Therapy
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Cyclophosphamide / administration & dosage
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Deoxyadenosines / administration & dosage
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Disease Progression
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Drug Resistance, Neoplasm
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Fatal Outcome
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Humans
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Interferon-alpha / administration & dosage
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Leukemia, Hairy Cell / classification
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Leukemia, Hairy Cell / complications
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Leukemia, Hairy Cell / drug therapy*
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Leukemia, Hairy Cell / surgery
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Male
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Neoplasms, Second Primary / classification
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Neoplasms, Second Primary / complications
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Neoplasms, Second Primary / drug therapy*
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Prednisolone / administration & dosage
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Recurrence
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Red-Cell Aplasia, Pure / drug therapy
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Red-Cell Aplasia, Pure / etiology*
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Remission Induction
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Rituximab
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Splenectomy
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Urinary Bladder Neoplasms / radiotherapy
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Murine-Derived
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Antineoplastic Agents
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Deoxyadenosines
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Interferon-alpha
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2-Chloroadenosine
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Rituximab
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Cyclophosphamide
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Prednisolone
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2-chloro-3'-deoxyadenosine